Microbiota-Brain-Gut Axis and Neurodegenerative Diseases

Diet rapidly and reproducibly alters the human gut microbiome

David, L. A., Maurice, C. F., Carmody, R. N., Gootenberg, D. B., Button, J. E., Wolfe, B. E., Ling, A. V., Devlin, A. S., Varma, Y., Fischbach, M. A., et al. (2014) · Nature · doi:10.1038/nature12820 · Cited by 10,100

Human gut microbiome viewed across age and geography

Yatsunenko, T., Rey, F. E., Manary, M. J., Trehan, I., Dominguez-Bello, M. G., Contreras, M., Magris, M., Hidalgo, G., Baldassano, R. N., Anokhin, A. P., et al. (2012) · Nature · doi:10.1038/nature11053 · Cited by 7,815

Dietary Modulation of the Human Colonic Microbiota: Introducing the Concept of Prebiotics

Gibson, G. R., & Roberfroid, M. B. (1995) · Journal of Nutrition · doi:10.1093/jn/125.6.1401 · Cited by 7,659

Enterotypes of the human gut microbiome

MetaHIT Consortium (additional members), Arumugam, M., Raes, J., Pelletier, E., Le Paslier, D., Yamada, T., Mende, D. R., Fernandes, G. R., Tap, J., Bruls, T., et al. (2011) · Nature · doi:10.1038/nature09944 · Cited by 7,548

Linking long-term dietary patterns with gut microbial enterotypes

Wu, G. D., Chen, J., Hoffmann, C., Bittinger, K., Chen, Y.-Y., Keilbaugh, S. A., Bewtra, M., Knights, D., Walters, W. A., Knight, R., et al. (2011) · Science · doi:10.1126/science.1208344 · Cited by 6,513

Inflamm‐aging: An Evolutionary Perspective on Immunosenescence

FRANCESCHI, C., BONAFÈ, M., VALENSIN, S., OLIVIERI, F., DE LUCA, M., OTTAVIANI, E., & DE BENEDICTIS, G. (2000) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2000.tb06651.x · Cited by 5,358

Ingestion of Lactobacillus strain regulates emotional behavior and central GABA receptor expression in a mouse via the vagus nerve

Bravo, J. A., Forsythe, P., Chew, M. V., Escaravage, E., Savignac, H. M., Dinan, T. G., Bienenstock, J., & Cryan, J. F. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1102999108 · Cited by 3,888

The Human Intestinal Microbiome in Health and Disease

Lynch, S. V., & Pedersen, O. (2016) · New England Journal of Medicine · doi:10.1056/nejmra1600266 · Cited by 3,637

Gut microbiota regulate motor deficits and neuroinflammation in a model of Parkinson's disease

Sampson, T. R., Debelius, J. W., Thron, T., Janssen, S., Shastri, G. G., Ilhan, Z. E., Challis, C., Schretter, C. E., Rocha, S., Gradinaru, V., et al. (2016) · Cell · doi:10.1016/j.cell.2016.11.018 · Cited by 3,622

Indigenous bacteria from the gut microbiota regulate host serotonin biosynthesis

Yano, J. M., Yu, K., Donaldson, G. P., Shastri, G. G., Ann, P., Ma, L., Nagler, C. R., Ismagilov, R. F., Mazmanian, S. K., & Hsiao, E. Y. (2015) · Cell · doi:10.1016/j.cell.2015.02.047 · Cited by 3,614

Dietary Flaxseed and Flaxseed Oil Differentially Modulate Aspects of the Microbiota Gut–Brain Axis Following an Acute Lipopolysaccharide Challenge in Male C57Bl/6 Mice

Livingston, D. B. H., Sweet, A., Rodrigue, A. F., Kishore, L., Loftus, J., Ghali, F., Mahmoodianfard, S., Celton, C., Hosseinian, F. S., & Power, K. A. (2023) · Nutrients · doi:10.3390/nu15163542 · Cited by 15

Immune Remodeling during Aging and the Clinical Significance of Immunonutrition in Healthy Aging

Dou, L., Yang, P., Zhang, B., Yang, H., & Zheng, K. (2023) · Aging and Disease · doi:10.14336/ad.2023.0923 · Cited by 14

Fecal Microbiota Transplantation in Amyotrophic Lateral Sclerosis: Clinical Protocol and Evaluation of Microbiota Immunity Axis

Niccolai, E., Martinelli, I., Quaranta, G., Nannini, G., Zucchi, E., Maio, F. D., Gianferrari, G., Bibbò, S., Cammarota, G., Mandrioli, J., et al. (2024) · Methods in molecular biology · doi:10.1007/978-1-0716-3662-6_27 · Cited by 15

Microbiota‐immune‐brain interactions: A new vision in the understanding of periodontal health and disease

Breivik, T. J., Gjermo, P. E., Gundersen, Y., Opstad, P. K., Murison, R. C. C., Hugoson, A., von Hörsten, S., & Fristad, I. (2024) · Periodontology 2000 · doi:10.1111/prd.12610 · Cited by 15

Iron Homeostasis Dysregulation, Oro-Gastrointestinal Microbial Inflammatory Factors, and Alzheimer’s Disease: A Narrative Review

Kuziak, A., Heczko, P. B., Pietrzyk, A., & Strus, M. (2025) · Microorganisms · doi:10.3390/microorganisms13010122 · Cited by 15

Reshaping the gut microbiota: Tangliping decoction and its core blood-absorbed component quercetin improve diabetic cognitive impairment

Zhang, W., Yi, C., Song, Z., Yu, B., Jiang, X., Guo, L., Huang, S., Xia, T., Huang, F., Yan, Y., et al. (2025) · Phytomedicine · doi:10.1016/j.phymed.2025.156560 · Cited by 15

The Relationship between Platelet Count and Host Gut Microbiota: A Population-Based Retrospective Cross-Sectional Study

Yoon, H., Kim, H., Lee, S. H., Kim, S. J., Chang, Y., Ryu, S., Shin, H., Kim, H., & Lee, J. H. (2019) · Journal of Clinical Medicine · doi:10.3390/jcm8020230 · Cited by 15

Pharmaceutically Active Microbial AhR Agonists as Innovative Biodrugs in Inflammation

Puccetti, M., Pariano, M., Costantini, C., Giovagnoli, S., & Ricci, M. (2022) · Pharmaceuticals · doi:10.3390/ph15030336 · Cited by 15

Bridging the Gap between Gut Microbiota and Alzheimer’s Disease: A Metaproteomic Approach for Biomarker Discovery in Transgenic Mice

Ayan, E. B., DeMirci, H., Serdar, M. A., Palermo, F., & Baykal, A. T. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241612819 · Cited by 15

Advances in the role of gut microbiota in the regulation of the tumor microenvironment (Review)

Xinyuan, T., Yu, L., Jianping, S., Rongwei, Z., Ruiwen, S., Ye, Z., Zhao, J., Chun-fang, T., Hongwei, C., & Haibin, G. (2023) · Oncology Reports · doi:10.3892/or.2023.8618 · Cited by 14

Fecal Microbiota Transplantation-Mediated Ghrelin Restoration Improves Neurological Functions After Traumatic Brain Injury: Evidence from 16S rRNA Sequencing and In Vivo Studies

Zhang, Y., Liu, J., Liu, X., Zhou, Y., Geng, J., Shi, Z., & Ma, L. (2023) · Molecular Neurobiology · doi:10.1007/s12035-023-03595-2 · Cited by 14

Gut–Kidney–Heart: A Novel Trilogy

Caldarelli, M., Franza, L., Rio, P., Gasbarrini, A., Gambassi, G., & Cianci, R. (2023) · Biomedicines · doi:10.3390/biomedicines11113063 · Cited by 14

Olfactory Three-Needle Electroacupuncture Improved Synaptic Plasticity and Gut Microbiota of SAMP8 Mice by Stimulating Olfactory Nerve

Wang, Y., Zheng, A.-N., Yang, H., Wang, Q., Dai, B., Wang, J., Wan, Y.-T., Liu, Z., & Liu, S. (2023) · Chinese Journal of Integrative Medicine · doi:10.1007/s11655-023-3614-3 · Cited by 14

Gut-brain axis interacts with immunomodulation in inflammatory bowel disease

Ye, X., Zhang, M., Zhang, N., Wei, H., & Wang, B. (2023) · Biochemical Pharmacology · doi:10.1016/j.bcp.2023.115949 · Cited by 15

Commensal Enterococcus faecalis W5 ameliorates hyperuricemia and maintains the epithelial barrier in a hyperuricemia mouse model

Liu, X., Han, C. H., Lei, K., Mao, T., Yu, Q., Li, C., Ke, L., Wu, J., Guo, Y., Zhang, W., et al. (2023) · Journal of Digestive Diseases · doi:10.1111/1751-2980.13249 · Cited by 14

IUPHAR review: From gut to brain: The role of gut dysbiosis, bacterial amyloids, and metabolic disease in Alzheimer’s disease

Inan, S., Wilson, R. P., & Tükel, Ç. (2025) · Pharmacological Research · doi:10.1016/j.phrs.2025.107693 · Cited by 15

Observation of the Gut Microbiota Profile in C57BL/6 Mice Induced by Plasmodium berghei ANKA Infection

Guan, W., Yang, S., Zhao, Y., Cheng, W., Song, X., Yao, Y., Xie, Y., Du, W., & Li, J. (2021) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2021.680383 · Cited by 14

Engineering Organoids for in vitro Modeling of Phenylketonuria

Borges, A. C., Broersen, K., Leandro, P., & Fernandes, T. G. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2021.787242 · Cited by 14

Exercise Preconditioning Ameliorates Cognitive Impairment in Mice with Ischemic Stroke by Alleviating Inflammation and Modulating Gut Microbiota

Lv, H., Wang, S., Tian, M., Wang, L., Gao, J., Zhao, Q., Li, Z., Jia, X., & Yu, Y. (2022) · Mediators of Inflammation · doi:10.1155/2022/2124230 · Cited by 14

Bifidobacterium promotes retinal ganglion cell survival by regulating the balance of retinal glial cells

Zhao, X., Xu, M., Zhao, Z., Wang, Y., Liu, Y., Zhang, T., Wan, X., Jiang, M., Luo, X., Shen, Y., et al. (2023) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.14165 · Cited by 14

Signal Pathways and Intestinal Flora through Trimethylamine N-oxide in Alzheimer's Disease

Zhang, Y., & Jian, W. (2023) · Current Protein and Peptide Science · doi:10.2174/1389203724666230717125406 · Cited by 14

The Microbiome–Neurodegeneration Interface: Mechanisms, Evidence, and Future Directions

Böckels, L., Alexa, D., Antal, D. C., Gațcan, C., Alecu, C., Kacani, K., Cretu, R. A., Piseru, E.-A., Bîlcu, R. V., & Cuciureanu, D. I. (2026) · Cells · doi:10.3390/cells15020135 · Cited by 13

Microbiota-gut-brain axis impairment in the pathogenesis of stroke: implication as a potent therapeutic target

Muhammad, M., Muchimapura, S., & Wattanathorn, J. (2023) · Bioscience of Microbiota Food and Health · doi:10.12938/bmfh.2022-067 · Cited by 14

The fecal microbiota from children with autism impact gut metabolism and learning and memory abilities of honeybees

Li, Y., Zhang, Y., Luo, X., Meng, Y., Zhong, Z., Zheng, H., & Yang, Y. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1278162 · Cited by 13

A long journey to treat epilepsy with the gut microbiota

Li, Q., Gu, Y., Liang, J., Yang, Z., & Qin, J. (2024) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2024.1386205 · Cited by 13

Understanding neurotropic enteric viruses: routes of infection and mechanisms of attenuation

Lulla, V., & Sridhar, A. (2024) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-024-05450-6 · Cited by 13

The Effect of Gut Microbe Dysbiosis on the Pathogenesis of Alzheimer's Disease (AD) and Related Conditions

Nafady, M. H., Sayed, Z. S., Abdelkawy, D. A., Shebl, M. E., Elsayed, R. A., Ashraf, G. M., Perveen, A., Attia, M. S., & Bahbah, E. I. (2022) · Current Alzheimer Research · doi:10.2174/1567205019666220419101205 · Cited by 13

Global trends in research on irritable bowel syndrome and the brain–gut axis: Bibliometrics and visualization analysis

Wu, P.-N., Xiong, S., Zhong, P., Yang, W., Chen, M., & Tang, T. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.956204 · Cited by 13

Gut microbiome-based therapies for alleviating cognitive impairment: state of the field, limitations, and future perspectives

Bu, L., Wang, C., Bai, J., Song, J., Zhang, Y., Chen, H., & Suo, H. (2024) · Food & Function · doi:10.1039/d3fo02307a · Cited by 13

Recent progresses in gut microbiome mediates obstructive sleep apnea‐induced cardiovascular diseases

Zhang, X., Zhang, H., Li, S. C., Fang, F., Yin, Y., & Wang, Q. (2024) · FASEB BioAdvances · doi:10.1096/fba.2023-00153 · Cited by 13

Association of dietary live microbe intake with various cognitive domains in US adults aged 60 years or older

Lv, J.-J., Li, X., Wang, J.-B., Yang, X., Yin, M.-Y., & Yang, C.-H. (2024) · Scientific Reports · doi:10.1038/s41598-024-51520-x · Cited by 13

Unravelling the potential of gut microbiota in sustaining brain health and their current prospective towards development of neurotherapeutics

Banerjee, A., Pradhan, L. K., Sahoo, P. K., Jena, K. K., Chauhan, N. R., Chauhan, S., & Das, S. K. (2021) · Archives of Microbiology · doi:10.1007/s00203-021-02276-9 · Cited by 13

Evaluating the Effects of Diet-Gut Microbiota Interactions on Sleep Traits Using the UK Biobank Cohort

Qi, X., Ye, J., Wen, Y. F., Liu, L., Cheng, B., Cheng, S., Yao, Y., & Zhang, F. (2022) · Nutrients · doi:10.3390/nu14061134 · Cited by 13

The microbiomes of the eyelid and buccal area of patients with uveitic glaucoma

Shin, J. H., Lee, J. W., Lim, S., Yoon, B. W., Lee, Y., & Seo, J. H. (2022) · BMC Ophthalmology · doi:10.1186/s12886-022-02395-x · Cited by 13

The Risk of Epilepsy after Long-term Proton Pump Inhibitor Therapy

Liang, C., Bai, Y., Hsu, J.-W., Huang, K., Ko, N., Tsai, C., Yeh, T., Chu, H., Tsai, S., Chen, T., et al. (2021) · Seizure · doi:10.1016/j.seizure.2021.03.008 · Cited by 13

Effects of common plastic products heat exposure on cognition: Mediated by gut microbiota

Hu, N., Pan, D., Yang, Y. H., Pu, L., He, X., Wang, H., Zhang, X., Du, Y., Yu, Z., He, S., et al. (2023) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2023.114758 · Cited by 12

Could the Urease of the Gut Bacterium Proteus mirabilis Play a Role in the Altered Gut–Brain Talk Associated with Parkinson’s Disease?

Grahl, M. V. C., Andrade, B. D. S., Perin, A. P. A., Neves, G. A., Duarte, L. D. S., Uberti, A. F., Hohl, K. S., Follmer, C., & Carlini, C. R. (2023) · Microorganisms · doi:10.3390/microorganisms11082042 · Cited by 12

The Role of Gut Microbiota in Neuromyelitis Optica Spectrum Disorder

Yao, S., Yang, X., Cen, L., & Tan, S. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25063179 · Cited by 12

Bifidobacterium infantis and Bifidobacterium breve Improve Symptomatology and Neuronal Damage in Neurodegenerative Disease: A Systematic Review

Reiriz, M., Beltrán-Velasco, A. I., Echeverry‐Alzate, V., Miguel, E. M., Gómez-Senent, S., Uceda, S., & Clemente‐Suárez, V. J. (2025) · Nutrients · doi:10.3390/nu17030391 · Cited by 12

Beyond weight loss: exploring the neurological ramifications of altered gut microbiota post-bariatric surgery

Almheiri, R. T., Hajjar, B. M., Alkhaaldi, S. M. I., Rabeh, N., Aljoudi, S., Abd‐Elrahman, K. S., & Hamdan, H. (2025) · Journal of Translational Medicine · doi:10.1186/s12967-025-06201-2 · Cited by 12

Encapsulation of L. fermentum with chitosan-alginate enhances its bioactivity against acrylamide toxicity in D.mel

Kumar, S. S., & Mohideen, S. S. (2025) · Scientific Reports · doi:10.1038/s41598-025-95499-5 · Cited by 12

Effect of the probiotic Escherichia coli Nissle 1917 on serum levels of NADPH oxidase-2 and lipopolysaccharide in patients with Alzheimer's disease

Loffredo, L., Alfano, A. R., Ettorre, E., Desideri, G., Carnevale, R., Forte, M., Maglione, V., Bartimoccia, S., Castellani, V., Totè, C. M., et al. (2025) · Journal of Alzheimer s Disease · doi:10.1177/13872877251345157 · Cited by 12

Gut microbiota and Parkinson’s disease: exploring pathogenesis and potential therapeutic strategies from a gut-brain axis perspective

Jin, X., Wei, J., Min, X., Fan, Y., Yuan, Z., Du, Z., Su, Z., Xun, T., Du, Q., Liang, T., et al. (2025) · iScience · doi:10.1016/j.isci.2025.114185 · Cited by 15

Leveraging microbiome-based interventions to improve the management of neurodegenerative diseases: evidence for effects along the microbiota-gut-brain axis

Auclair‐Ouellet, N., Kassem, O., Bronner, S., Oula, M.-L., & Binda, S. (2025) · Frontiers in Nutrition · doi:10.3389/fnut.2025.1699884 · Cited by 12

Appetite Suppression and Interleukin 17 Receptor Signaling Activation of Colonic Mycobiota Dysbiosis Induced by High Temperature and High Humidity Conditions

Guo, Y., Guo, H., Qiu, L., Fu, Y., Zhu, X., Zhang, H., Wang, J., & Chen, D. (2021) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2021.657807 · Cited by 12

Gut microbiota modulation by prednisolone in a rat kindling model of pentylenetetrazol (PTZ)-induced seizure

de Lima, A. M. D. L., Rosa, G. D. L., Guzzo, E. F. M., Padilha, R. B., da Silva, R. C., Silveira, A. K., Morales, D. D. L., de Araujo, M. C., Moreira, J. C. F., Barth, A. L., et al. (2021) · Microbial Pathogenesis · doi:10.1016/j.micpath.2021.105376 · Cited by 12

Exploration of acupuncture therapy in the treatment of mild cognitive impairment based on the brain-gut axis theory

Jin, Y., Hu, F., & Zhu, J. (2022) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2022.891411 · Cited by 12

Correlates of Zonulin and Claudin-5, markers of intestinal and brain endothelial permeability, in Parkinson's Disease: A pilot study

Ulaş, S. B., Aras, Y. G., Gözükara, S. I., Acar, T., & Acar, B. A. (2023) · Parkinsonism & Related Disorders · doi:10.1016/j.parkreldis.2023.105361 · Cited by 12

Exploring the alteration of gut microbiota and brain function in gender-specific Parkinson’s disease based on metagenomic sequencing

Zhang, M., Zhai, Z., Yang, B., He, L., Wang, J., Dai, W., Xue, L., Yang, X., Feng, Y., & Wang, H. (2023) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2023.1148546 · Cited by 12

A New Integrative Theory of Brain-Body-Ecosystem Medicine: From the Hippocratic Holistic View of Medicine to Our Modern Society

Guidolin, D., Anderlini, D., Maura, G., Marcoli, M., Cortelli, P., Buonaura, G. C., Woods, A. S., & Agnati, L. F. (2019) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph16173136 · Cited by 12

Correlation Between Gut Microbiome Composition and Acute Pain Perception in Young Healthy Male Subjects

Shiro, Y., Arai, Y.-C. P., Ikemoto, T., Ueda, W., & Ushida, T. (2020) · Pain Medicine · doi:10.1093/pm/pnaa401 · Cited by 12

Prebiotic Treatment Increases Serum Butyrate in People With Schizophrenia

Kelly, D. L., Kane, M. A., Fraser, C. M., Sayer, M. A., Grant-Beurmann, S., Liu, T., Gold, J. M., Notarangelo, F. M., Vyas, G. R., Richardson, C. M., et al. (2021) · Journal of Clinical Psychopharmacology · doi:10.1097/jcp.0000000000001364 · Cited by 12

Differences in the eyelid and buccal microbiome between open‐angle glaucoma and uveitic glaucoma

Lee, J. W., Lim, S., Shin, J. H., Lee, Y., & Seo, J. H. (2021) · Acta Ophthalmologica · doi:10.1111/aos.14967 · Cited by 12

Systemic Metabolism and Mitochondria in the Mechanism of Alzheimer’s Disease: Finding Potential Therapeutic Targets

Song, M., & Fan, X. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24098398 · Cited by 11

Gut–Brain Crosstalk and the Central Mechanisms of Orofacial Pain

Tao, R., Liu, S., Crawford, J. A., & Tao, F. (2023) · Brain Sciences · doi:10.3390/brainsci13101456 · Cited by 11

Exploring the Secrets of Microbes: Unveiling the Hidden World Through Microbial Omics in Environment and Health

Mallik, B., Mishra, T. K., Dubey, P., Kesheri, M., & Kanchan, S. (2024) · Springer eBooks · doi:10.1007/978-981-97-1769-9_10 · Cited by 11

Characterizing Gut Microbiota in Older Chinese Adults with Cognitive Impairment: A Cross-Sectional Study

Wang, J., Zhang, G., Lai, H., Li, Z., Shen, M., Li, C., Kwan, P., O'Brien, T. J., Wu, T., Yang, S., et al. (2024) · Journal of Alzheimer s Disease · doi:10.3233/jad-240597 · Cited by 11

Decoding TGR5: A comprehensive review of its impact on cerebral diseases

Zhang, Z., Zhang, Y., Peng, H., Yu, Q., Kang, X., Liu, Y., Zheng, Y., Cheng, F., Wang, X., & Li, F. (2025) · Pharmacological Research · doi:10.1016/j.phrs.2025.107671 · Cited by 11

Bacteria-derived 3-hydroxydodecanoic acid induces a potent anti-tumor immune response via the GPR84 receptor

Katkeviciutė, E., Bircher, A., Sanchez, R., Schwill, M., Dorst, A., Morsy, Y., Conde, J., Zamboni, N., Gademann, K., Scharl, M. M., et al. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.115357 · Cited by 11

Impact of Gut Microbiota and Probiotics on Rheumatoid Arthritis: A Potential Treatment Challenge

Ajith, T. A., & Anita, B. B. (2025) · International Journal of Rheumatic Diseases · doi:10.1111/1756-185x.70266 · Cited by 11

Brain Structure and Function: Insights from Chemical Neuroanatomy

Agnati, L. F., Guidolin, D., Cervetto, C., Maura, G., & Marcoli, M. (2023) · Life · doi:10.3390/life13040940 · Cited by 12

Gut microbiota and circadian rhythm in Alzheimer’s disease pathophysiology: a review and hypothesis on their association

Khezri, M. R., & Ghasemnejad‐Berenji, M. (2023) · npj Aging · doi:10.1038/s41514-023-00104-6 · Cited by 11

Abnormalities in Clostridioides and related metabolites before ACTH treatment may be associated with its efficacy in patients with infantile epileptic spasm syndrome

Wan, L., Shi, X., Yan, H., Liang, Y., Liu, X., Zhu, G., Zhang, J., Wang, J., Wang, M., & Yang, G. (2023) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.14398 · Cited by 11

Gastroesophageal reflux disease with 6 neurodegenerative and psychiatric disorders: Genetic correlations, causality, and potential molecular mechanisms

Zhan, Z., Huang, Z.-M., Zhou, H., Xie, Z., Chen, Y.-Z., Luo, Y., Chen, P., Kang, J., Cheng, Z. J., & Sun, B. (2024) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2024.02.030 · Cited by 11

A New Treatment Landscape for RCC: Association of the Human Microbiome with Improved Outcomes in RCC

Piao, X., Byun, Y. J., Zheng, C.-M., Song, S. J., Kang, H. W., Kim, W. T., & Yun, S. J. (2023) · Cancers · doi:10.3390/cancers15030935 · Cited by 11

Current Understanding of the Roles of Gut–Brain Axis in the Cognitive Deficits Caused by Perinatal Stress Exposure

Rubinstein, M. R., Burgueño, A. L., Quiroga, S., Wald, M. R., & Genaro, A. M. (2023) · Cells · doi:10.3390/cells12131735 · Cited by 11

Cannabidiol improves the cognitive function of SAMP8 AD model mice involving the microbiota-gut-brain axis

Ma, B.-Q., Jia, J., Wang, H., Li, S., Yang, Z.-J., Wang, X., & Yan, X.-S. (2024) · Journal of Toxicology and Environmental Health · doi:10.1080/15287394.2024.2338914 · Cited by 11

The Role of Microbiota in Upper and Lower Gastrointestinal Functional Disorders

Mandarino, F. V., Sinagra, E., Raimondo, D., & Danese, S. (2023) · Microorganisms · doi:10.3390/microorganisms11040980 · Cited by 11

Causal associations between inflammatory bowel disease and anxiety: A bidirectional Mendelian randomization study

He, Y., Chen, C.-L., He, J., & Liu, S.-D. (2023) · World Journal of Gastroenterology · doi:10.3748/wjg.v29.i44.5872 · Cited by 10

Shared Genetic Architecture Among Gastrointestinal Diseases, Schizophrenia, and Brain Subcortical Volumes

Xie, Y., Zhao, Y., Zhou, Y., Jiang, Y., Zhang, Y., Du, J., Cai, M., Fu, J., & Liu, H. (2024) · Schizophrenia Bulletin · doi:10.1093/schbul/sbae099 · Cited by 10

An update on mammalian and non-mammalian animal models for biomarker development in neurodegenerative disorders

Mishra, R., & Upadhyay, A. (2025) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-025-05668-y · Cited by 11

Gut microbiome regulation in equine animals: current understanding and future perspectives

Li, F., Kong, X., Khan, M. Z., Lin, W., Wei, J., Zhu, M., Liu, G., Huang, B., Wang, C., & Zhang, Z. (2025) · Frontiers in Microbiology · doi:10.3389/fmicb.2025.1602258 · Cited by 10

Protein Hydrolysates’ Absorption Characteristics in the Dynamic Small Intestine In Vivo

He, Y., Shen, L., Ma, C., Chen, M., Pan, Y., Yin, L., Zhou, J., Lei, X., Ren, Q., Duan, Y., et al. (2018) · Molecules · doi:10.3390/molecules23071591 · Cited by 10

Harnessing the Gut Microbiota to Potentiate the Efficacy of CAR T Cell Therapy

Gabrielli, G., Shouval, R., Ghilardi, G., van den Brink, M. R. M., & Ruella, M. (2023) · HemaSphere · doi:10.1097/hs9.0000000000000950 · Cited by 10

Association of Plastic Exposure with Cognitive Function Among Chinese Older Adults

Zhu, Y., Wu, Y., Shi, L., Yang, Y., Wang, Y., Pan, D., He, S., Wang, L., & Li, J. (2024) · Journal of Alzheimer s Disease · doi:10.3233/jad-240746 · Cited by 10

Gut microbiota: A new window for the prevention and treatment of neuropsychiatric disease

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